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Cellosaurus is database indexing available cell lines from various collections: American Type Culture Collection (ATCC), Bioresource Collection and Research Center, Taiwan (BCRC), Banco de Células do Rio de Janeiro (BCRJ), CellBank Australia (CBA), Collection of Cell Lines in Veterinary Medicine (CCLV), Cell Lines Service (CLS), Coriell, Drosophila Genomics Resource Center (DGRC), Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (DSMZ), European Bank for induced pluripotent Stem Cells (EBiSC), European Collection of Authenticated Cell Cultures (ECACC), Interlab Cell Line Collection (ICLC), Institute for Fermentation Osaka (IFO), Istituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia Romagna (IZSLER) biobank, Japanese Collection of Research Bioresources (JCRB) Cell Bank, Kunming Cell Bank of Type Culture Collection (KCB), Korean Cell Line Bank (KCLB), Millipore, National Cell Bank of Iran (NCBI_Iran), National Cancer Institute - Developmental Therapeutics Program (NCI-DTP), NINDS Human Cell and Data Repository (NHCDR), NIH AIDS Reagent Program (NIH-ARP), NISES, RIKEN Bioresource Center Cell Bank (RCB), Royan Stem Cell Bank (RSCB), Tick Cell Biobank (TCB), Tohoku University cell line catalog (TKG), and Ximbio.
https://web.expasy.org/cellosaurus/CVCL_1C71
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection.
Proper citation: RRID:CVCL_1C71 Copy
https://web.expasy.org/cellosaurus/CVCL_AZ13
Organism: Homo sapiens (Human)
Disease: Merosin-deficient congenital muscular dystrophy type 1A
Category: Transformed cell line
Proper citation: RRID:CVCL_AZ13 Copy
https://web.expasy.org/cellosaurus/CVCL_5K27
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Transformed cell line
Proper citation: Coriell Cat# GM24204, RRID:CVCL_5K27 Copy
https://web.expasy.org/cellosaurus/CVCL_AZ01
Organism: Homo sapiens (Human)
Disease: Merosin-deficient congenital muscular dystrophy type 1A
Category: Finite cell line
Proper citation: RRID:CVCL_AZ01 Copy
https://web.expasy.org/cellosaurus/CVCL_4T55
Organism: Homo sapiens (Human)
Disease: Ullrich congenital muscular dystrophy
Category: Transformed cell line
Proper citation: RRID:CVCL_4T55 Copy
https://web.expasy.org/cellosaurus/CVCL_1C71
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection.
Proper citation: Coriell Cat# GM24168, RRID:CVCL_1C71 Copy
https://web.expasy.org/cellosaurus/CVCL_4T63
Organism: Homo sapiens (Human)
Disease: Ullrich congenital muscular dystrophy
Category: Transformed cell line
Proper citation: RRID:CVCL_4T63 Copy
https://web.expasy.org/cellosaurus/CVCL_4T63
Organism: Homo sapiens (Human)
Disease: Ullrich congenital muscular dystrophy
Category: Transformed cell line
Proper citation: Coriell Cat# GM24237, RRID:CVCL_4T63 Copy
https://web.expasy.org/cellosaurus/CVCL_1C77
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection.
Proper citation: RRID:CVCL_1C77 Copy
https://web.expasy.org/cellosaurus/CVCL_1C77
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection.
Proper citation: Coriell Cat# GM24176, RRID:CVCL_1C77 Copy
https://web.expasy.org/cellosaurus/CVCL_AZ01
Organism: Homo sapiens (Human)
Disease: Merosin-deficient congenital muscular dystrophy type 1A
Category: Finite cell line
Proper citation: Coriell Cat# GM24218, RRID:CVCL_AZ01 Copy
https://web.expasy.org/cellosaurus/CVCL_AZ11
Organism: Homo sapiens (Human)
Disease: Merosin-deficient congenital muscular dystrophy type 1A
Category: Transformed cell line
Proper citation: RRID:CVCL_AZ11 Copy
https://web.expasy.org/cellosaurus/CVCL_Y785
Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line
Proper citation: RRID:CVCL_Y785 Copy
https://web.expasy.org/cellosaurus/CVCL_5K45
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: Coriell Cat# GM24292, RRID:CVCL_5K45 Copy
https://web.expasy.org/cellosaurus/CVCL_5K37
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Transformed cell line
Proper citation: Coriell Cat# GM24283, RRID:CVCL_5K37 Copy
https://web.expasy.org/cellosaurus/CVCL_5K48
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: Coriell Cat# GM24295, RRID:CVCL_5K48 Copy
https://web.expasy.org/cellosaurus/CVCL_5K56
Organism: Homo sapiens (Human)
Disease: Smith-Magenis syndrome
Category: Transformed cell line
Proper citation: RRID:CVCL_5K56 Copy
https://web.expasy.org/cellosaurus/CVCL_5K34
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: Coriell Cat# GM24279, RRID:CVCL_5K34 Copy
https://web.expasy.org/cellosaurus/CVCL_5K38
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: RRID:CVCL_5K38 Copy
https://web.expasy.org/cellosaurus/CVCL_5K45
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: RRID:CVCL_5K45 Copy
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